Canonical Allele Identifier: CA2060730386
Gene: CASC18 HGNC NCBI

Linked Data

dbSNP Id: rs1869967115

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.105714738A>G , CM000674.2:g.105714738A>G GRCh38
NC_000012.11:g.106108516A>G , CM000674.1:g.106108516A>G GRCh37
NC_000012.10:g.104632646A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110108.1:n.54+10482A>G
NR_110109.1:n.55-424A>G
NR_110110.1:n.83+7882A>G
NR_110111.1:n.83+7882A>G
NR_110111.2:n.83+7882A>G